Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
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01 2PCAS Ecully FR
02 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
03 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
04 1EXCELLA GMBH & CO. KG Feucht DE
05 1FAREVA LA VALLEE Saint-Germain-Laprade FR
06 1FDC Limited Mumbai IN
07 1MICRO LABS LIMITED Bengaluru IN
08 1OLON S.P.A. Rodano IT
09 1Ven PetroChem & Pharma (India) Pvt Ltd Mumbai IN
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01 9Timolol maleate
02 1Timolol maleate, Process II
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01 2France
02 1Germany
03 4India
04 1Israel
05 1Italy
06 1Luxembourg
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01 10Valid
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : CEP 2014-300 - Rev 01
Status : Valid
Issue Date : 2023-09-27
Type : Chemical
Substance Number : 572
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 1998-147 - Rev 11
Status : Valid
Issue Date : 2022-03-24
Type : Chemical
Substance Number : 572
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : CEP 1996-049 - Rev 07
Status : Valid
Issue Date : 2023-10-16
Type : Chemical
Substance Number : 572
Certificate Number : CEP 2010-084 - Rev 03
Status : Valid
Issue Date : 2023-10-19
Type : Chemical
Substance Number : 572
Certificate Number : R1-CEP 2001-296 - Rev 05
Status : Valid
Issue Date : 2023-07-05
Type : Chemical
Substance Number : 572
Certificate Number : CEP 2021-304 - Rev 00
Status : Valid
Issue Date : 2024-04-24
Type : Chemical
Substance Number : 572
Certificate Number : R1-CEP 2003-070 - Rev 03
Status : Valid
Issue Date : 2020-09-15
Type : Chemical
Substance Number : 572
Certificate Number : R0-CEP 2022-322 - Rev 00
Status : Valid
Issue Date : 2023-06-28
Type : Chemical
Substance Number : 572
Certificate Number : R1-CEP 2003-239 - Rev 05
Status : Valid
Issue Date : 2021-03-16
Type : Chemical
Substance Number : 572
Certificate Number : R1-CEP 2005-065 - Rev 00
Status : Valid
Issue Date : 2012-05-24
Type : Chemical
Substance Number : 572
A Timolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Timolol, including repackagers and relabelers. The FDA regulates Timolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Timolol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Timolol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Timolol supplier is an individual or a company that provides Timolol active pharmaceutical ingredient (API) or Timolol finished formulations upon request. The Timolol suppliers may include Timolol API manufacturers, exporters, distributors and traders.
click here to find a list of Timolol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Timolol CEP of the European Pharmacopoeia monograph is often referred to as a Timolol Certificate of Suitability (COS). The purpose of a Timolol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Timolol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Timolol to their clients by showing that a Timolol CEP has been issued for it. The manufacturer submits a Timolol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Timolol CEP holder for the record. Additionally, the data presented in the Timolol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Timolol DMF.
A Timolol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Timolol CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Timolol suppliers with CEP (COS) on PharmaCompass.
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